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72594-86-6

BENZYL TERT-BUTYL MALONATE

Catalog#: AR003OTN  |   CAS#: 72594-86-6  |   MDL#: MFCD01075175  |   MF: C14H18O4  |   MW: 250.29032

Packsize Purity Price Availability Quantity
1g 97% $4.00 Global Stock Buy Now Add To Cart
5g 97% $10.00 Global Stock Buy Now Add To Cart
10g 97% $15.00 Global Stock Buy Now Add To Cart
25g 97% $28.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003OTN
Chemical Name BENZYL TERT-BUTYL MALONATE
CAS Number 72594-86-6
Molecular Formula C14H18O4
Molecular Weight 250.29032
MDL Number MFCD01075175
SMILES O=C(CC(=O)OC(C)(C)C)OCc1ccccc1

Benzyl tert-butyl malonate is a versatile compound widely used in chemical synthesis due to its unique properties. This compound serves as a key building block in organic chemistry, particularly in the formation of various organic compounds. Its application in chemical synthesis includes:1. **Acylation Reactions**: Benzyl tert-butyl malonate can undergo acylation reactions, where the benzyl group or t-butyl group can be selectively modified to introduce specific functional groups. This allows chemists to control the reactivity and selectivity of the compound in various synthetic pathways.2. **Medicinal Chemistry**: Benzyl tert-butyl malonate is often employed in the synthesis of pharmaceutical intermediates and active ingredients. Its structural versatility and reactivity make it a valuable precursor for creating new drug candidates with improved biological activities.3. **Polymer Chemistry**: This compound can be utilized in polymerization reactions to introduce malonate functionalities into polymers, enhancing their properties such as solubility, adhesion, and mechanical strength. It acts as a monomer in certain polymerization processes, leading to the formation of novel polymeric materials.4. **Protecting Group Strategies**: The tert-butyl ester functionality in Benzyl tert-butyl malonate can serve as a protecting group for sensitive functional groups during chemical transformations. By selectively deprotecting the tert-butyl ester under mild conditions, chemists can access reactive sites within a molecule without causing unwanted side reactions.5. **Cross-Coupling Reactions**: Benzyl tert-butyl malonate can participate in cross-coupling reactions with various organometallic reagents, enabling the formation of complex molecular structures in a controlled manner. This reactivity is valuable in the construction of carbon-carbon and carbon-heteroatom bonds in the synthesis of natural products and fine chemicals.
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